Possible mechanisms underlying copper-induced damage in biological membranes leading to cellular toxicity.

Abstract It is generally accepted that copper toxicity is a consequence of the generation of reactive oxygen species (ROS) by copper ions via Fenton or Haber–Weiss reactions. Copper ions display high affinity for thiol and amino groups occurring in proteins. Thus, specialized proteins containing clusters of these groups transport and store copper ions, hampering their potential toxicity. This mechanism, however, may be overwhelmed under copper overloading conditions, in which copper ions may bind to thiol groups occurring in proteins non-related to copper metabolism. In this study, we propose that indiscriminate copper binding may lead to damaging consequences to protein structure, modifying their biological functions. Therefore, we treated liver subcellular membrane fractions, including microsomes, with Cu 2+ ions either alone or in the presence of ascorbate (Cu 2+ /ascorbate); we then assayed both copper-binding to membranes, and microsomal cytochrome P450 oxidative system and GSH-transferase activities. All assayed sub-cellular membrane fractions treated with Cu 2+ alone displayed Cu 2+ -binding, which was significantly increased in the presence of Zn 2+ , Hg 2+ , Cd 2+ , Ag +1 and As 3+ . Treatment of microsomes with Cu 2+ in the μM range decreased the microsomal thiol content; in the presence of ascorbate, Cu 2+ added in the nM concentrations range induced a significant microsomal lipoperoxidation; noteworthy, increasing Cu 2+ concentration to ≥50 μM led to non-detectable lipoperoxidation levels. On the other hand, μM Cu 2+ led to the inhibition of the enzymatic activities tested to the same extent in either presence or absence of ascorbate. We discuss the possible significance of indiscriminate copper binding to thiol proteins as a possible mechanism underlying copper-induced toxicity.